Celerity 20 Steam Process Challenge Device for Dynamic Air Removal Cycles— 510(k) K173626
Substantially EquivalentSTERIS Corporation
FDA 510(k) clearance K173626 for Celerity 20 Steam Process Challenge Device for Dynamic Air Removal Cycles, Substantially Equivalent on 2018-02-21. Applicant: STERIS Corporation. Device class: 2.
Clearance details
- Applicant
- STERIS Corporation
- Product code
- Code FRC
- Device class
- Class 2
- Regulation
- 21 CFR 880.2800
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mentor, OH, US
Recent devices under product code FRC
view allMore clearances from STERIS Corporation
view allRecalls naming K173626
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K173626.
Data sourced from openFDA. This site is unofficial and independent of the FDA.